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Medicine in DR Congo · official US FDA label

Unipur 0.546% éq 2.178

Chlore (chlorine) · poudre

Authorized in DR Congo

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This is a US label.

The official US FDA label for chlorine, effective July 15, 2025, describes products sold in the United States. The medicine sold in DR Congo may differ in strength, form or approved uses: ask a pharmacist or a doctor.

Official US FDA label for chlorine

Data provided by the U.S. Food and Drug Administration (openFDA), unchanged. The full label on DailyMed.

Uses

Uses: See symptoms on front panel. Relieves hoarseness *

Dosage

US dosage, for products sold in the United States. For a medicine bought in DR Congo, follow its box, its leaflet or your pharmacist.

Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

Where to find it in DR Congo

Not in stock in our pharmacies right now

Stock changes with every sale. Search by substance: a medicine with the same composition may be available.

Composition

SubstanceStrengthATC code
Chlore (chlorine)0.546% éq 2.178—

Marketing authorization in DR Congo

From the register of the ACOREP (the Congolese pharmaceutical regulatory authority).

  • Authorization number

    MS.1253/10/05/DGM/961/2022

    Valid from July 26, 2022 until July 26, 2027

    Holder
    UNIQUE PHARMA Av. Bakongo n° 17, commune de Gombe, ville de Kinshasa, R.D Congo
    Manufacturer
    HIND PHARMA 11-G, Industrial Area, Govindpura, Bhopal-462022, India
    Country
    Inde

Sources

  • ●Labels: U.S. Food and Drug Administration, openFDA (public domain). Data provided by the U.S. Food and Drug Administration (openFDA), unchanged. DailyMed.
  • ●English names of substances: RxNorm, U.S. National Library of Medicine.
  • ●Marketing authorizations: register of the ACOREP, DR Congo, version of February 4, 2026.

Public information, for reference only: it does not replace the advice of a pharmacist or a doctor. Vimpia writes nothing about how to use a medicine and translates nothing: the label is the US FDA's, unchanged; names, composition and authorizations come from the official sources above.